A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075834



Internal ID19325709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54526080..54552081hg38UCSC Ensembl
chr11:51567199..51593200hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3826002
hg1926002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771155
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075834
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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